IRCT201102071310N7已完成2 期
Randomized trial to determination of minimal dose of Lidocaine with Sufentanil‘s fixed dose in spinal anesthesia for cesarean section.
Vice Chancellor for Research Kermanshah University of Medical Sciences0 个研究点目标入组 126 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 126
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20 years 至 35 years（—）
- 性别
- Female
入选标准
- •Exclusion criteria: All patients who are not class I and II ASA; Patients not signed the informed consent; Patients with underlying disease; Patients with chronic pain or; Who have used analgesic medications in the past forty eight hours; Patients with abscess or local infection at the injection site; Severe agitation; Cerebral disorder; Severe psychological disorders and addiction;
排除标准
- 未提供
研究者
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